Disease #00458 (DMBCYP2D6 (metabolism, drug, poor/rapid), OMIM:608902)

Official abbreviation DMBCYP2D6
Name metabolism, drug, poor/rapid
OMIM ID 608902
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene CYP2D6
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Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00033751 - PubMed: Gough 1990 - - - United Kingdom (Great Britain) - - 0 - - DMBCYP2D6 poor metaboliser CYP2D6 CYP2D6 7 1 Johan den Dunnen
00033753 - PubMed: Steen 1995 - - - - (not applicable) - - 0 - - DMBCYP2D6 - CYP2D6 CYP2D6 1 1 Johan den Dunnen
00033754 - - reference haplotype - - - (not applicable) - - 0 - - DMBCYP2D6 poor metaboliser (debrisoquine, sparteine) CYP2D6 CYP2D6 1 1 Johan den Dunnen
00033755 - PubMed: Gough 1990 - - - United Kingdom (Great Britain) - - 0 - - DMBCYP2D6 poor metaboliser CYP2D6 CYP2D6 1 1 Johan den Dunnen
00033756 - PubMed: Hanioka 1990 - - - ? (unknown) - - 0 - - DMBCYP2D6 poor metaboliser CYP2D6 CYP2D6 8 1 Johan den Dunnen
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